K, Rb, Cs, Sr and Ba contents and Sr isotope ratios of ocean floor basalts

Reliable analyses of K, Rb and Cs in dredge basalts require samples which show no petrographic evidence of alteration minerals and which have H 2 O + contents less than 0.7 %. Very fresh glass samples usually have H 2 O + levels of 0.1 to 0.2 %, and this probably represents the primary level of H 2 O in most submarine basalt magmas. A dredge haul containing both basalt and andesite was studied for major element and trace element variations. The major elements were consistent with a differentiation model involving crystallization of plagioclase, olivine, clinopyroxene and titanomagnetite. This differentiation had little effect on Sr concentration and on K/Rb and K/Cs ratios; these parameters are thus especially useful in studying mantle chemistry and partial melting processes. Twenty-eight unaltered dredge basalts were analysed, with K/Rb ratios varying from 360 to 1350. K contents of most samples, after correction for high level (shallow) differentiation processes, fall in the range 500 to 1200 parts/10 6 . A comparison of unaltered basalts from ‘fast-spreading ridges’ and ‘slowspreading ridges’ shows that K, Rb, Cs and Sr contents and K/Rb, K/Cs and Rb/Sr ratios are identical for both environments, while Ba contents and 87 Sr/ 86 Sr ratios may be significantly different. Thus mantle chemistry appears to be largely decoupled from the dynamic processes of plate movement. It is shown that submarine ridge basalts have lower 87 Sr/ 86 Sr ratios than the basalts of the oceanic islands, suggesting an early depletion of parts of the mantle in the dispersed elements. Average values for 15 samples from 11 different ridge localities: K = 1160 parts/10 6 ; Rb = 1.11 parts/ 10 6 ; Cs = 0.016 parts/10 6 ; Sr = 135 parts/10 6 ; Ba = 10 parts/10 6 ; K/Rb = 1060; K/Cs = 70000; Rb/Sr = 0.0082; 87 Sr/ 86 Sr = 0.70265.

Author(s):  
Corey A. Honl ◽  
Ryan M. Rudnitzki

The following paper describes the release of the 220GL engine and APG2000/3000 Enginator™ product lines from Waukesha Engine. The major elements of the release that will be covered include the installation and calibration of the ESM® control system, the development of new capabilities to control fuel injection and its associated features, the integration of Waukesha-introduced components on the 220GL, high-level product strategy and justification, and early stage performance figures from development testing.


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pp. 4584-4611 ◽  
Author(s):  
Milena Marjanović ◽  
Suzanne M. Carbotte ◽  
Hélène D. Carton ◽  
Mladen R. Nedimović ◽  
Juan Pablo Canales ◽  
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Author(s):  
Jörg Hasenclever ◽  
Sonja Theissen-Krah ◽  
Lars H. Rüpke ◽  
Jason P. Morgan ◽  
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1991 ◽  
Vol 42 (4) ◽  
pp. 409 ◽  
Author(s):  
WW Ahlers ◽  
JP Kim ◽  
KA Hunter

The spatial distributions of the dissolved trace metals Cu, Ni, Cd, Zn and Pb and of reactive Hg have been measured in parallel with the major elements Na, K, Mg and Ca and electrical conductivity in three sampling events in the Manuherikia River, New Zealand. The geographical span of the sampling sites ranged from a pristine subalpine upper catchment area through lower altitude sites that are increasingly affected by both natural weathering processes and moderate agricultural and domestic runoff. Major-element concentrations in the upper catchment were at or below the 1% frequency minimum of the spectrum of global river compositions, indicating a highly pristine system. Concen- trations increased steadily downstream to levels similar to world average river water. All trace metals exhibited the same spatial trends as the major ions. Typical upper-catchment concentrations were very low by global standards: Cu (150 ng L-1), Ni (100-150 ng L-1), Cd (8 ng L-I), Zn (150-200 ng L-1), Pb (20-30 ng L-1) and Hg (0.3 ng L-1). Oceanic residence times calculated from the data for Zn (80 000 years) and Cd (230 000 years) for which few reliable estimates have been made, are consistent with observed correlations between the oceanographic distributions of these elements and dissolved silicon or phosphate, respectively.


2010 ◽  
Vol 160 (5) ◽  
pp. 683-704 ◽  
Author(s):  
Lydéric France ◽  
Juergen Koepke ◽  
Benoit Ildefonse ◽  
Sarah B. Cichy ◽  
Fabien Deschamps

2011 ◽  
Vol 311 (3-4) ◽  
pp. 275-286 ◽  
Author(s):  
Sonja Theissen-Krah ◽  
Karthik Iyer ◽  
Lars H. Rüpke ◽  
Jason Phipps Morgan

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